HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94852585_94852586insGGCG , CM000672.2:g.94852585_94852586insGGCG | GRCh38 |
NC_000010.10:g.96612342_96612343insGGCG , CM000672.1:g.96612342_96612343insGGCG | GRCh37 |
NC_000010.9:g.96602332_96602333insGGCG | NCBI36 |
NG_008384.2:g.94880_94881insGGCG | |
NG_008384.3:g.94905_94906insGGCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.1292-148_1292-147insGGCG MANE Select | ENSP00000360372.3:n.1292-148_1292-147insGGCG | |
ENST00000645461.1:n.2203-148_2203-147insGGCG | ||
ENST00000371321.7:c.1292-148_1292-147insGGCG | ENSP00000360372.3:n.1292-148_1292-147insGGCG | |
ENST00000464755.1:c.2055-148_2055-147insGGCG | ENSP00000483243.1:n.2055-148_2055-147insGGCG | |
NM_000769.2:c.1292-148_1292-147insGGCG | NP_000760.1:n.1292-148_1292-147insGGCG | |
NM_000769.4:c.1292-148_1292-147insGGCG MANE Select | NP_000760.1:n.1292-148_1292-147insGGCG |